EVO-DEVO
Heterochrony: the Evolution of Development
Kenneth J. McNamara
Published online: 5 June 2012
#Springer Science+Business Media, LLC 2012
Abstract Heterochrony can be defined as change to the timing or rate of development relative to the ancestor. Because organisms generally change in shape as well as increase in size during their development, any variation to the duration of growth or to the rate of growth of different parts of the organism can cause morphological changes in the descendant form. Heterochrony takes the form of both increased and decreased degrees of devel-opment, known as “peramorphosis” and “paedomorpho-sis,” respectively. These are the morphological consequences of the operation of processes that change the duration of the period of an individual’s growth, either starting or stopping it earlier or later than in the ancestor, or by extending or contracting the period of growth. Heterochrony operates both intra- and interspe-cifically and is the source of much intraspecific varia-tion. It is often also the cause of sexual dimorphism. Selection of a sequence of species with a specific het-erochronic trait can produce evolutionary trends in the form of pera- or paedomorphoclines. Many different life history traits arise from the operation of heterochronic processes, and these may sometimes be the targets of selection rather than morphological features themselves. It has been suggested that some significant steps in evolution, such as the evolution of vertebrates, were engendered by heterochrony. Human evolution was fuelled by heterochrony, with some traits, such as a large brain, being peramorphic, whereas others, such as reduced jaw size, are paedomorphic.
Keywords Evolution . Heterochrony . Paedomorphosis . Peramorphosis . Sexual dimorphism . Evolutionary trends
Introduction
Lurking deep in Darwin’s monumental tomeOn the Origin of Species, first published in 1859 (Darwin1859), is a short, much neglected, section. Lying between pages 439 and 450 in the first edition and between pages 386 and 396 in my copy of the sixth edition published in 1878 is the kernel of some ideas that were intermittently to surface in the field of evolutionary theory for the following 150 years. These insights now form a major part of modern evolutionary theory. The section in question was entitled“Embryology” by Darwin in the first edition, but“Development and Em-bryology” in the sixth, and highlights the importance to evolution of changes to the pattern of an organism’s onto-genetic development.
Darwin’s (1878, p. 386) view of development and em-bryology was that,“This is one of the most important sub-jects in the whole round of natural history.”But his ideas on the significance of these intrinsic aspects of evolutionary theory are scattered through much of the book and form the basis for many of Darwin’s ideas on what generates the variation that is the raw material upon which natural selec-tion operates. Darwin was undoubtedly influenced by ideas that had been around since the early nineteenth century and promulgated by embryologists like von Baer in Germany and Serres in France (see Gould 1977). Darwin (1878, p. 396) encapsulated these ideas by observing that, “Embryol-ogy rises greatly in interest, when we look at the embryo as a picture, more or less obscure, of the progenitor, either in its adult or larval state, of all members of the same great class.” K. J. McNamara (*)
Department of Earth Sciences, University of Cambridge, Downing Street,
Evolution was perceived as having proceeded by an increase in complexity and an increase in the extent of ontogenetic change, by terminal addition. This idea was to be encapsulated by a great adherent of Darwin’s concept of natural selection, Ernest Haeckel (1866), who wrote that, “Ontogeny is the brief and rapid recapitulation of phylogeny dependent on the physiological functions of heredity (repro-duction) and adaptation (nutrition).” Within the develop-mental history of a single individual, it was believed, lay the entire evolutionary history of the group. Each animal or plant was perceived as a repository of all that had gone before—an infinite number of evolutionary Russian dolls.
But to Darwin, developmental change was not always unidirectional, leading to more complex forms. Darwin rec-ognized that there were many instances when species had evolved that had undergone less developmental change than their ancestors:“…some animals are capable of reproducing at a very early age, before they have acquired their perfect characters; and if this power became thoroughly well devel-oped in a species, it seems probable that the adult stage of development would sooner or later be lost; and in this case, especially if the larva differed much from the mature form, the character of the species would be greatly changed and degraded.”(Darwin1878, p. 149).
These views presaged ideas that resurfaced in the 1920s and were articulated by the English embryologist Walter Garstang, who argued that vertebrates could have evolved from something as inconsequential as the larva of a tunicate (sea squirt). This tadpole-like juvenile possesses many of the attributes present in adult vertebrates (see below) (Garstang 1928). To get his point across, Garstang was moved to express his ideas about this phenomenon in the Mexican salamander, or axolotl (Fig. 1), in verse:
Ambystoma's a giant newt who rears in swampy waters,
As other newts are wont to do, a lot of fishy daughters: These Axolotls, having gills, pursue a life aquatic,
But, when they should transform to newts, are naughty and erratic.
They change upon compulsion, if the water grows too foul,
For then they have to use their lungs, and go ashore to prowl:
But when a lake's attractive, nicely aired, and full of food,
They cling to youth perpetual, and rear a tadpole brood.
And newts Perrenibranchiate have gone from bad to worse:
They think aquatic life is bliss, terrestrial a curse. They do not even contemplate a change to suit the weather,
But live as tadpoles, breed as tadpoles, tadpoles all together!
What Garstang argued was that major evolutionary changes (including the evolution of vertebrates themselves) could have arisen from such arrested development and re-tention of ancestral juvenile traits by descendant adults. Garstang called this paedomorphosis. It was quite the op-posite to what Haeckel had suggested, his so-called “reca-pitulation.”With the rise in importance of genetics in the early twentieth century, the role of developmental change in evolution all but disappeared from the literature.
But, in 1977, in his seminal bookOntogeny and Phylog-eny, Steven J. Gould argued that not only was developmen-tal change a fundamendevelopmen-tal aspect of evolution but that the two “forms,”paedomorphosis and recapitulation, both oc-curred: development could slow down or speed up, or be shortened or prolonged, in the descendent relative to the ancestor. This is what generated much of the raw material for natural selection to work on and reflected ideas articu-lated by Darwin about 120 years earlier, but largely forgotten.
Darwin, though, was not one for using jargon, and I suspect that it is for this reason that his insights have been neglected. Gould was at the forefront of the renaissance in recent years in the relationship between development and evolution. Although subsequently touted as the “new” as-pect of evolutionary theory in the guise of evolutionary developmental biology, many of the old ideas that Gould and others espoused in the 1970s and 1980s had been amal-gamated under the banner of“heterochrony,”a term coined by Haeckel. This formed the basis for the resurgence in interest in the role of developmental change in evolution, which has seen a profusion of papers on developmental genetics to explain many of the changes seen in the phenotype.
Until the 1970s, evolution was thought to center on the classical Darwinian paradigm of natural selection and
genetics: genes provide the mutations on which natural selection operates. However, the publication of Gould’s Ontogeny and Phylogenyhighlighted the added significance of developmental changes in evolution. Much of the early research in this field was carried out by paleontologists in the 1980s, focusing on macroevolutionary changes resulting from heterochrony (see McKinney 1988; McKinney and McNamara1991; McNamara1995a, 1997). In the 1990s, an increasing number of biologists began to recognize the importance of developmental change in evolution (Hall 1992).
What Is Heterochrony?
Heterochrony can be defined as“change to the timing or rate of developmental events, relative to the same events in the ancestor”(Alberch et al. 1979; McKinney and McNamara 1991). All organisms have an ontogeny. This is their life history, from the time of conception until death. While organisms increase in size as they grow, from an initial egg, through larval or embryonic stages, to juvenile and then adult stages, they also change in shape. You, for in-stance, look very different now from what you looked like when you were born, for the simple reason that many parts of your body have changed in relative shape during your ontogeny. Most organisms have a finite period of growth, which usually ends at the onset of sexual maturity, both size and shape slowing down markedly, or stopping. Within populations of a single species, individuals do not all grow and develop at the same rate or for the same duration; individuals grow at slightly different rates and for slightly different durations. The same holds for many species, where, between closely related species, the main morpho-logical differences arise from variations to the rate and duration of growth.
Certain parts of a single individual may grow for relatively different lengths of time and at different relative rates. Thus, in many vertebrates, for instance, the rate of growth of the head is relatively greater than growth of the trunk or limbs during the embryonic phase of growth, whereas after birth, these post-cranial parts undergo a relatively greater amount of growth. Likewise, the formation of finger bones in dolphins can arise from an extension of the period of growth of these parts of the limbs (Richardson and Oelschläger 2002). Thus, slight changes to the rate or duration of growth of various parts of the body during ontogeny can greatly impact upon the appear-ance of the final adult form. All such changes to the rate and duration of growth of all or part of an organism compared with its ancestor are what define heterochrony.
An organism’s growth is determined by its genetic makeup. The genes determine, to a large degree, its morphological, physiological, and behavioral characteristics—so what it
looks like, how it functions, and how it behaves. It is now recognized that developmental genes, particularly those regu-lating embryonic or larval development, play a major role in evolution (Richardson and Brakefield 2003). One group of genes known as homeotic genes controls the timing of expres-sion of growth factors that determine when and where a particular morphological structure starts to develop and its duration of growth. Thus, any changes to the timing of ex-pression of these controlling genes, or the period during which they influence growth, will result in a descendant that can look markedly different from its immediate ancestor.
Any genes that control the regulation of development are now collectively known as “heterochronic genes.” Slack and Ruvkun (1998, p. 375) wrote that,“Genes that control the temporal dimension of development, heterochronic genes, can be thought of as the temporal analogs of the homeotic genes, which regulate spatial dimensions (e.g., anterior-posterior, dorsal-ventral axes) during development of metazoans. These pathways generate graded or binary levels of regulatory factors that pattern one axis of the developing animal. Heterochronic genes may be the target of mutations that cause heterochronic change in phylogeny.” Subtle morphological changes therefore occur continual-ly within populations, arising from slight variations between individuals in the duration and rate of growth of the whole organism, or of just particular traits. Within populations, this produces so-called intraspecific variation: heterochronic change being targeted by natural selection. Because hetero-chrony is so important in providing raw material on which natural selection can operate, it plays a very important role in evolution (McKinney and McNamara1991; McNamara 1995a, b, 1997; Tills et al. 2011). As well as operating within species at this level of intraspecific variation, it also occurs between sexes (McNamara1995b); between species, in generating evolutionary trends (McNamara 1982,1990); and in the evolution of major morphological novelties, such as vertebrates and birds (McNamara 1997; McNamara and McKinney2005).
Classifying Heterochrony
development and is said to show peramorphosis. Frequently, though certainly not inevitably, paedomorphic forms may be smaller than their ancestor, while peramorphic forms tend to be larger. Paedomorphosis and peramorphosis arenot evo-lutionary processes in themselves but are descriptive terms that describe the appearance of the descendant morphology. They are the morphological (and sometimes behavioral) end result of the operation of a variety of heterochronic processes.
Paedomorphosis and peramorphosis can each be pro-duced by three different, complementary processes: varia-tions in time of cessation of growth, variation in time of commencement of growth, and change in rate of growth (Alberch et al. 1979; McNamara 1986a). Paedomorphosis occurs if the period of growth of the descendant form is stopped prematurely—progenesis(hypomorphosisof Reilly et al. 1997); if onset of growth is delayed— postdisplace-ment; or if the rate of growth is less in the descendant than in the ancestor—neoteny (deceleration of Reilly et al. 1997) (Figs.2and3). Progenesis will affect the entire organism if premature cessation of growth is caused by the earlier onset of sexual maturity. Like neoteny and postdisplacement, it may, though, also target specific morphological features.
Peramorphosis occurs if the period of growth in the descendant is extended (hypermorphosis), if the onset of growth occurs earlier in the descendant than in the ancestor (predisplacement), or if the growth rate is increased ( accel-eration). Hypermorphosis, like progenesis, can affect the whole organism when the onset of sexual maturity is delayed, because fast juvenile growth rates will persist for a longer period. Alternatively, hypermorphosis can target just certain traits. Acceleration and predisplacement will affect only specific features, not the entire organism.
While this categorization of heterochrony into these six basic processes appears to have much utility, it has been argued that this presupposes a uniformity of morphological change during ontogeny, which may not always be the case (Rice1997). It is often possible to compartmentalize ontog-eny into discrete growth phases, such as embryonic,
infantile, and juvenile growth in mammals, or discrete growth instars in arthropods. Each of these phases can have its own ontogenetic trajectory, which might be at variance with other growth phases. Each can be subjected to its own heterochronic variation, involving extensions or contrac-tions of these phases, or discrete variation in growth rates. This type of intra-ontogenetic heterochrony is called se-quential heterochrony(McNamara2002).
The terminology of heterochrony can be used to describe the appearance of discrete structures formed during ontoge-ny, such as the number of vertebrae or digits (so-called “meristic”characters) that develop during ontogeny. It can also be applied to the subsequent changes in shape of these structures during growth. These have been termed mitotic and growth heterochrony, respectively (McKinney and McNamara 1991). In many organisms, mitotic hetero-chrony, particularly that induced by pre- and postdisplace-ment, can play a very significant role during very early developmental stages. This is due to variations between ancestors and descendants in the timing of onset of devel-opment of major morphological features. Neoteny and ac-celeration, in other words reduced and accelerated growth rates, respectively, will be especially common during later ontogenetic development.
The relationship between size and shape is known as allometryand arises from differential growth rates between different parts of the body or in different axes on the same structure. For instance, as a bone grows, it may become relatively longer and thinner because growth is occurring at a faster rate along one axis than another. Should the relative size and shape of a structure remain the same throughout ontogeny, relative to the organism’s overall body size, growth is described as isometric. Although very few organisms grow isometrically (Klingenberg 1998), some individual traits, such as vertebrate skeletal elements, can be isometric. Usually, though, a structure such as a bone will change shape and size relative to the size and shape of the whole organism during ontogeny. If the bone increases in relative size, growth is said to occur by positive allometry.
However, if there is a relative reduction in size, growth is said to shownegative allometry.
There is a close relationship between allometry and het-erochrony because hethet-erochrony involves changes not only in time but also in shape and size. The consequence of changing growth rates (acceleration and neoteny) is to cause
such allometric changes. Extensions or contractions of the period of growth–in other words, hypermorphosis or pro-genesis–have the effect of accentuating or reducing the effects of allometric changes. Consequently, those organ-isms that undergo pronounced allometric change during growth are more likely to generate very different descendant
Fig. 3 A hypothetical animal which, during its ontogeny, undergoes a number of morphological changes. Peramorphic descendants develop
“beyond”the ancestor; padomorphic descendants retain juvenile an-cestral features. In hypermorphosis, growth stops later; in acceleration, the horns and tails grow faster; in predisplacement, the horns and tail
adult morphologies if rates or durations of growth have changed.
For example, when the skull of the domestic dog,Canis familiaris, is compared with that of the domestic cat,Felis domestica, the dog skull can be seen to undergo pronounced positive allometric change during ontogeny, particularly by strong growth of the muzzle (Fig.4). By artificially chang-ing growth rates and timchang-ing, a wide range of breeds that vary substantially in cranial morphology have been produced. For instance, tiny dogs like chihuahuas or King Charles spaniels are very paedomorphic, but large Irish wolfhounds are peramorphic (Fig.5). In contrast, the extent of allometric change is minimal in the domestic cat, so that breeds do not differ greatly in morphology (Wayne1986). In the natural world, the same effect occurs. Those organisms that produce a wider range of variation because of greater ontogenetic allometric change produce more raw material for natural
selection, leading to the evolution of a wide range of descendants.
It may be trifle hard to imagine but your fluffy little Pekingese dog peering at you with doting eyes is really a wolf. This is because, as one of the numerous breeds of domestic dog (many unwittingly selected for by humans for particular heterochronic traits), it“evolved”from a wolf. All the traits present in the first known domestic dogs, which date back to at least 30,000 years (Germonpré et al.2009), occur in puppies of wolves: shortened muzzles; steeper, wider foreheads; and smaller body size (Fig. 6). Thus, domestic dogs are essentially paedomorphic wolves (Morey 1994). But Mesolithic man was unlikely to have been selecting for these traits. He was more likely to have been selecting aspects of juvenile wolf behavior. Such more ame-nable juvenile behavior is more likely to have put wolf pups in contact with humans. Socialization in dogs is best devel-oped when they are between three and 12 weeks old, at a time when primary bonds are formed. Those that fail to
Fig. 4 Proportionate differences in skull shapes of domestic dogs and cats as they grow up. Dogs undergo much greater shape changes than do cats. This explains the greater diversity of skull shapes in different breeds of dogs, compared with cats. Modified and redrawn from Wayne (1986)
bond with humans are likely to have been driven away or killed.
Identifying Heterochrony
Recognizing the effect of heterochronic processes requires knowledge of ontogenetic information from both ancestral and descendant forms. Whereas many ontogenetic changes will be species specific, there are many general changes that occur within particular groups of higher taxa, so that even if the ontogeny of the descendant and presumed ancestral form are not known in detail, a number of inferences concerning likely occurrence of heterochrony can still be made. Many examples of heterochrony have been documented in the fossil record (McNamara 1995a, 1997). When dealing with fossil material, two of the factors involved in heterochrony, namely shape and size, are always available. As such, it is possible to assess whether a particular species is either peramorphic or paedomor-phic. However, understanding which processes have caused the heterochrony can be difficult when dealing with fossil material, as accurate details of the duration of rate of growth are often unknown.
However, one group that can provide such information is dinosaurs. A number of studies have been made describing growth rates and time of onset of sexual maturity and cessation or reduction in growth in dinosaurs (McNamara and Long2012). For instance, studies of bone microstruc-ture in a range of dinosaurs show that periodic, possibly seasonal, growth is reflected in growth lines in the bone (see
below). This allows“real”-time information to be obtained from such fossil material, making it possible to produce relatively accurate inferences of the type of heterochronic processes operating in extinct species.
Many paleontological studies have used size as a proxy for time—that is, if one species is smaller than another, it is assumed that it grew for a shorter period of time. Conse-quently, assumptions are made that, for example, a descen-dant that is smaller than its ancestor and shows paedomorphic morphological characteristics, ceased growing at an earlier age and therefore arose by progenesis. So, for instance, the small late Cretaceous tyrannosaurid dinosaur, Maleevosau-rus, which was “only”five meters long, is smaller than its presumed ancestor but also possesses some paedomorphic features. As I have pointed out, paedomorphosis can be caused by neoteny or progenesis. Either process could ex-plain paedomorphosis in these smaller tyrannosaurs. Howev-er, studies in other groups of organisms show that neoteny tends to target only specific structures, not the whole organ-ism. In the case of Maleevosaurus, although progenesis is more probable, in the absence of actual growth rate data, it is not possible to determine the process precisely.
While it may often seem to be relatively straightforward to identify heterochrony, such as a reduction or increase in number of segments in adults of different species of trilo-bites (Fig.8), identifying subtle allometric changes between ancestor and descendant may be less obvious. One tech-nique used in a number of studies is morphometrics. Here, fixed positions (known as landmarks) on, say, a trilobite head, are recorded for different ontogenetic stages. These are then compared with the same positions on a presumed descendant species. Subtle variations in growth rates of parts
of the structure will occur by heterochronic processes that can be identified (e.g., Webster et al.2001). Mitteroecker et al. (2005) have applied this technique to a study of the evolution of cranial growth in chimpanzees. However, they caution against the use of single characters when trying to interpret heterochrony. Rather, they argue (Mitteroecker et al.2005, p. 255), “…that a single morphological characterization, descriptions in terms of bigger/smaller or more/less of some-thing, should generally not be subjected to heterochronic interpretation, nor should single ratios. Multivariate analysis circumvents this theoretical problem when heterochrony is defined as multivariate ontogenetic scaling along a common ontogenetic trajectory.”
Relative Frequency of Heterochrony
It has been argued that theoretically, paedomorphosis and peramorphosis should occur with roughly equal frequencies (Gould1977). Yet studies of heterochrony in the fossil record suggest that this may not always be the case. Amphibians show a preponderance of paedomorphosis (McNamara1988), which may be related to their large cell size, causing a reduced rate of cellular division (McNamara1997).
Paedomorphosis has occurred many times in frogs, for example, resulting in the development of many miniature species. The 29 smallest species (with the smallest having an average body length of just 7.7 millimeters) are spread across five families and 11 genera (Rittmeyer et al.2012). As well as very reduced size, these frogs have reduced fecundity and show paedomorphic traits of reduced
ossification and lack of digits. Moreover, many of these frogs are direct developers, lacking a tadpole stage, and as such form a distinct ecological guild (Rittmeyer et al.2012). In contrast, peramorphosis may have been more frequent in dinosaurs, in particular being a major contributing factor to the evolution of very large body size (McNamara and Long 2012). Many types of dinosaurs, such as sauropods, ceratop-sians, theropods, and ornithopods, show not only trends to-ward increased body size but also the attainment of larger, more complex morphologies by peramorphosis (Fig.7).
Heterochrony played a very important role in the evolu-tion of trilobites. This is thought to have been due to their developmental systems having been poorly constrained when they first evolved in the Early Cambrian (McNamara 1986b). This is shown by the high variability in segment number, both within and between species in these earliest trilobites. Through Cambrian times, there is progressive improvement in the trilobites’ developmental systems, so that by post-Cambrian times, many families of trilobites have fixed thoracic segment number. Moreover, documented cases indicate that in Cambrian trilobites, natural selection favored paedomorphic processes more than peramorphic ones (Fig. 8). However, greater morphological diversity of post-Cambrian trilobites may have been facilitated by a shift to selection for mainly peramorphic processes.
Heterochrony and Sexual Dimorphism
Many species of animals exhibit sexual dimorphism. This can take the form of differences in average maximum size
between males and females and/or differences in morpho-logical features. This size and morphomorpho-logical variance arises from either variations in growth rates or differences in the relative times of onset of sexual maturity; in other words, it arises from heterochrony (see, for example, the work by Denoël et al. (2009) on European newts). A relative modest example occurs in the Indian Ocean blue boxfish, Strophiur-ichthys robustus, where both male and female juveniles have a diamond-shaped body and a body pattern dominated by spots. During their development, males change their body shape, so that it becomes more oval in outline. This probably reflects a change in their degree of maneuverabil-ity when swimming. Their body pattern also changes from spots to a series of elongate wavy patterns. The females, however, retain the juvenile features of diamond-shaped body and body pattern of spots (Fig.9). Thus, the females can be regarded as paedomorphic, compared with the males (McNamara1995b).
A more extreme case occurs in deep sea angler fish, such asPhotocorynus, where the male is very much smaller than the female, retains early juvenile morphological features,
and lives parasitically attached to the female’s head (McNamara 1997, p. 116). Perhaps one of the most extreme examples of sexual dimorphism is in eulimid gastropods. These animals live parasitically within holothuroids (sea cucumbers). The males are exceedingly reduced in size and complexity and themselves live within the body of the female where they live attached to a special receptacle and grow to be little more than a testis (Fig.10). Such extreme dimorphism, of a smaller, paedomor-phic male living within or upon a female, is not that uncommon in marine invertebrates, examples having been documented in a number of groups of mollusks and echinoderms. Many exam-ples of less extreme sexual dimorphism brought about by heterochrony have been described in primates, in particular in macaques (German et al.1994).
Many species of beetles develop very enlarged front legs, mandibles, horns, or other protruding structures on their head. These are the product of positive allometry and so are more well developed in larger individuals that have grown for longer. Frequently, males grow for longer periods than females during development and end up possessing these prominent structures while females do not (McNamara
1995b). Sometimes, even within a single sex, this character may be dimorphic. Cook (1987) showed that one of the sexual dimorphic characters in the dung beetleOnthophagus feroxare the horns, which occur on the males but not the females. Even here, there are two distinctive male morphs,
one with a small body size and lacking horns, the other larger and with horns. Such male dimorphism, arising from allometric scaling of horn size, occurs in a number of other beetles and shows that such horns form due to differences in either growth rates or timing of cessation of growth, in conjunction with strong positive allometry in the structure. A similar example occurs in the New Zealand tree weta Hemideina crassidens (Kelly and Adams 2010), two male morphs differing in head weaponry, which is reduced in females, the differences rising from variations to duration of growth during ontogeny.
How big a beetle grows and thus whether or not the male develops large structures are partly dependent on availabil-ity of food. Brown and Lockwood (1986) found that in the forked fungus beetleBolitotherus cornutus, individuals that as larvae feed on more nutritious fungi emerge as adults at a larger size and attain a larger adult size. Consequently, the males form relatively larger horns than individuals feeding on less nutritious fungi. Moreover, even the developmental state of the fungus can affect the beetle’s growth rates. So beetle larvae feeding on younger fungi grow faster and attain a larger body size than those feeding on older fungi that are less nutritious.
Heterochrony and the Evolution of Large Body Size
The pattern of evolutionary trends of increased body size that occurs very frequently in the fossil record is known as Cope's rule (Hone and Benton 2005). It is probable that peramorphosis is a prime factor in generating such increases in body size, either by hypermorphosis or acceleration (McNamara 1997). Studies of lineages of Jurassic bivalves
Fig. 9 The adult female of the blue boxfishStropiurichthys robustusis paedomorphic compared with the male, resembling the juvenile in body shape and body patterning. Reproduced with permission from McNamara (1997)
and ammonites (Hallam1975) demonstrated that many show trends to increased body size. Similar patterns occur in foraminifers, primates, and other mammals (McKinney in McNamara 1990) and in pterosaurs (Hone and Benton 2007).
The effect of peramorphosis in driving trends of in-creased body size is best shown by dinosaurs (McNamara and Long 2012). The peramorphic trends of increases in body size in sauropods, ceratopsians, theropods, and orni-thopods produced not only increases in body size, but also increased complexity of many morphological features (Fig.7). Recent research on bone microstructure has shown that many juvenile dinosaurs experienced very rapid growth rates (Padian et al.2001; Sander and Klein2005), implying that acceleration was the process responsible for the attain-ment of the peramorphic features. However, studies of the-ropod growth patterns support the argument that the evolution of very large body sizes of many dinosaurs may have occurred by a combination of both acceleration and hypermorphosis.
In a study of tyrannosaurid theropods, growth rate data for four genera,Albertosaurus,Gorgosaurus,Daspletosaurus, and Tyrannosaurus, were compared (Erickson et al.2004). Alber-tosaurusandGorgosaurusare the smallest,Daspletosaurusa little larger, andTyrannosaurusappreciably the largest. Using bone histology, it was calculated that the body size of Tyran-nosauruswas about 5.5 tons. It grew fastest for about the first four years of its life, when it was adding about two kilograms per day. Growth slowed after that until full maturity was reached when the dinosaur was about 18.5 years old.
The other three theropods were relatively smaller, reaching maximum body sizes of about one ton inGorgosaurusand Albertosaurus, and about 1.5 tons inDaspletosaurus. Their maximum growth rates also persisted for up to about four years but were much less than inTyrannosaurus rex, being about one-third to one-half kilogram per day. These genera would have also become mature at a younger age thanT. rex, between about 14 and 16 years. So not only was T. rex growing much faster (acceleration) than other tyrannosaurids, but it also had a delayed offset of growth (hypermorphosis). When these four tyrannosaurids are compared with geologi-cally older theropods, such as Syntarsus, the earlier forms became mature at the much younger age of about four years and had a maximum growth rate of only nine kilograms per year (Chinsamy1990). It is significant that the evolution of gigantism in other reptiles, notably crocodiles and lizards, was attained only by hypermorphosis (Erickson et al.2003).
Heterochrony and Developmental Trade-Offs
Most organisms are not just paedomorphic or peramorphic but a mixture of traits that evolved by both peramorphic and
paedomorphic processes. Such a mixture is known as dis-sociated heterochrony. It has been suggested that there may be a relationship between the peramorphic and paedomor-phic traits, such that the paedomorpaedomor-phic traits may be devel-opmental trade-offs for the peramorphic features (McNamara 1997). For instance, peramorphosis and size increase are often associated with the development of some paedomorphic traits. Evolutionary trends toward increased body size result in the organisms being required to input a greater amount of energy to attain the larger body and the accompanying more complex morphological featurers than in ancestral forms. This can be achieved by trade-offs, with selection pressure preferentially favoring some structures.
A classic example of a developmental trade-off is the dinosaurT. rexwhich as well having a huge body, possessed extremely reduced paedomorphic forelimbs and a hand with only two digits. This paedomorphic forelimb of T. rex is very unlikely to have had any adaptive significance but may have been a developmental trade-off for the evolution of its large body size, particularly the hind limbs and the head. The peramorphic development of a large body size in com-bination with increased complexity and size of the skull and hind limbs is offset by the paedomorphic reduction in the forelimbs and digits.
This phenomenon has also been recognized in hominid evolution, where it is known as the “expensive tissue hy-pothesis”(Aiello and Wheeler1995). Here, while selection has favored larger body size and brain in humans by hyper-morphic extension of the growth period, the trade-off to evolve metabolically hungry brain tissue is the reduction of the size of the gut, the lower jaw, and teeth. Likewise, in large ratite birds such as the ostrich and emu, trends to a large body size and very large hind limbs are offset by a paedomorphic reduction in the wings and a flightless habit.
Heterochrony and Evolutionary Novelties
The reason that early maturation, or progenesis, has been proposed as potentially the most important heterochronic process to produce evolutionary novelties (Gould1977) is that progenesis involves not just the pronounced morpho-logical disparity between ancestor and descendant due to the much earlier offset of growth, but selection may also target the life history strategy of precocious maturation (see be-low) rather than morphology itself. However, other hetero-chronic processes, such as neoteny and hypermorphosis, may also play a significant role in macroevolution. A study of the largest-ever terrestrial lizard, the Australian Pleisto-cene varanidVaranus(Megalania)prisca, has shown how it evolved by hypermorphosis (Erickson et al. 2003). This giant reptilian carnivore, measuring about seven meters in length and weighing more than half a ton, was more than twice the length of any living varanid. It reached its enor-mous size by delaying its time of onset of maturity by three to four years compared with other varanids.
Limb loss in snakes and whales also demonstrates the importance of paedomorphosis in the evolution of morpho-logical novelties. Here again, rather than progenesis, the process is more likely to have been neoteny or postdisplace-ment, or perhaps a combination of the two. The apparent dominance of paedomorphosis in the evolution of major morphological novelties is due, in part, to the greater degree of morphological difference between very early embryonic and adult forms than between adult morphologies that have been accelerated or extended by hypermorphosis. Having said that, however, it may be that peramorphic changes very early in development, such as an earlier onset of growth of specific morphological traits, might play as significant a role in the formation of morphological novelties as paedomor-phic delays.
Sometimes, the evolution of a major new group of organ-isms can be attributed to dissociated heterochrony, with the evolution of critical paedomorphic and peramorphic traits combining to produce a radically different organism. A classic example of this is the evolution of birds from dino-saurs. It is now known from the superbly preserved Early Cretaceous dinosaurs of Liaoning in China that many small dinosaurs possessed feathers. It is feasible that feathers were also present not only on some small adult dinosaurs but also on juveniles of larger forms. If this was the case, then the small-bodied dinosaurs, such as the feathered Sinosaurop-teryxandCaudipteryx, can be interpreted as paedomorphic dinosaurs. Similarly, the retention of feathers in birds can be considered as being by paedomorphosis. Early birds that evolved in the Late Jurassic to Early Cretaceous show other paedomorphic traits, such as reduction in some digits; a small body size; retention of a number of unfused bones; a gracile, elongate skull; large orbit; and a relatively large brain case. However, a critical feature of early birds, such as Archaeopteryx, is the possession of greatly enlarged
forelimbs that enabled the development of flight. These formed by peramorphic processes targeting these particular skeletal elements.
Heterochrony and Evolutionary Trends
Heterochrony is also important in the generation of evolu-tionary trends (McNamara1982,1990). This is because the link between evolutionary trends and heterochrony is due to the inherent directionality in evolutionary trends that also occurs in organisms’ development. For an evolutionary trend to become established, selection of either more and more paedomorphic or peramorphic traits must take place along an environmental gradient. For instance, in the aquatic environment, this could be from deep to shallow water or from coarse- to fine-grained sediments. In the case of evo-lutionary trends generated by heterochrony in dinosaurs situated in the terrestrial environment, the agents of selec-tion are harder to quantify but may relate to “arms races” between predators and prey: as a prey species evolves a larger body size to combat the effect of predation from a particular source, so selection will favor larger predators.
Any evolutionary trend that shows increasingly more paedomorphic characters between ancestors to descendants is called apaedomorphocline. If increasingly more peramor-phic descendants evolve, it is called a peramorphocline (McNamara 1982). The driving force behind such hetero-chronically driven trends is generally either competition or predation pressure. When the trend forms by competition, the ancestral form will persist and force selection in a single direction, away from the ancestral species. However, selec-tion brought on by predaselec-tion pressure will produce anage-netic evolutionary trends, where ancestral species are progressively replaced by the descendant forms and do not persist. Examples of paedomorphoclines have been described in Cenozoic brachiopods (McKinney and McNamara1991), where the environmental gradient was from deep to shallow water (Fig. 11); in trilobites (McNamara 1986a); and in ammonoids (Dommergues1990; Korn 1995; Gerber2011). The best examples of peramorphoclines are in dinosaurs (McNamara and Long2012).
Heterochrony and Life History Strategies
most well known is the “r–K continuum.” This describes both environments and life history traits of the organisms that inhabit these environments. Despite ther–Kcontinuum model being an oversimplification of life history strategies, it appears to offer some applicability at higher taxonomic levels as well as containing many elements that fit with current ideas on density-dependent regulation, resource availability, and environmental fluctuations (see Reznick et al.2002for a review of the controversy over the use of the theory).
The“r-selected”end of the continuum consists of unpre-dictable, often ephemeral, environments. As a result, selec-tion pressure for organisms that inhabit such environments favors those that mature rapidly, have short life spans, and have small body size. These are all features of progenesis. Organisms that arer-selected typically produce large numb-ers of offspring. At the other end of ther–Kcontinuum are “K-selected”organisms that occupy predictable, stable envi-ronments. These organisms typically have a relatively delayed onset of reproduction, long life span, and conse-quent large body size, all features of hypermorphosis. Such organisms produce few, large offspring. In addition to being generated by progenesis,r-selected characteristics may also be produced by acceleration (McKinney and McNamara 1991). Moreover, many K-selected organisms appear to
Fig. 11 Over a period of about 60 million years, the
Australasian brachiopods TegulorhynchiaandNotosaria have become increasingly paedomorphic, forming an evolutionary trend in the form of a paedomorphocline. The retention of more
paedomorphic features has allowed successive species to colonize increasingly shallow water. The earliest forms inhabited deep, quiet water. The species at the end of the paedomorphocline inhabits the intertidal zone. Reproduced with permission from McNamara (1997)
show some traits that evolved by neoteny, as well as hyper-morphosis, so a reduction in growth rate rather than a delay in offset of maturity.
A good example of the role of heterochrony in the evo-lution of life history strategies occurs in the kangaroo mouse, kangaroo rat, and pocket gopher that live in North America (Fig.12). Natural selection did not favor the length of their tail, color of their fur, nor size of their eyes, but the life history strategy of the animals. It used to be argued that the evolution in these heteromyid rodents of morphological features such as big hind feet, large eyes, and long tail was an adaptation to a life in the desert, the large head counter-balancing the rodent as it hopped purposefully through the cool desert nights on large sand-paddle feet, hunting for food using its big eyes and steering with the large rudder-like tail (McKinney and McNamara1991).
However, research by Hafner and Hafner (1988) indi-cates that the small size and paedomorphic traits of the adult kangaroo mouse Microdipodops were due to selection for the earlier maturation, producing a body length of just eight centimeters. By contrast, the adult of the larger kangaroo rat Dipodomysevolved by a reduction in rate of development. This genus has a longer life span, slower development, larger body size (20-centimeter length), longer gestation period, and smaller litters than the mouse. These are classic K-selected features. A third, related rodent, the pocket go-pher Orthogeomys, grows to about a third of a meter in length. But instead of retardation of growth, there has been a hypermorphic extension of the growth period, producing a robust body form.
Extrinsic factors such as climate change can have a direct impact on life history traits in some types of plants by inducing heterochronic changes in descendants. Studies of evolutionary change in the annual plantBrassicacollected in California before and after a five-year drought found that these drought conditions produced many changes in descen-dant life history traits that relate to changes to timing of development (Franks and Weis 2008). These include a change to earlier flowering time, as well as longer duration of flowering. These descendants also had thinner stems and fewer leaf nodes at flowering time than ancestral forms, showing that the result of the drought was selection for plants that flowered at a smaller size and at an earlier ontogenetic stage instead of selecting for plants that just developed more rapidly.
Conclusions
For the last half-billion years, this Earth has been populated by an astounding menagerie of organisms. Millions of spe-cies have come and gone—they have evolved; they have gone extinct. What has enabled this great panoply of forms
to evolve has been the inherent flexibility within the ge-nomic systems of organisms that has enabled subtle varia-tions to take place within populavaria-tions in the rate of growth and variations in the timing of initiation and cessation of growth. Controlled by critical heterochronic genes that switch growth on and off at different times and the genes that control the growth hormones that dictate the extent to which particular traits will develop, evolution of morpholo-gy and consequently, behavior, is very much determined by heterochrony.
But what of you and me? Is there any reason why we too shouldn’t also have had our evolutionary histories molded by the all-pervasive influence of heterochrony? No reason at all. As far back as the 1920s, it was being suggested that many of our morphological features appeared to be charac-teristic of juvenile apes: our flat faces, reduced body hair, relatively large brains housed in thin skull bones, absence of brow ridges, and reduced jaw with too many teeth. These features would all seem to indicate that we are paedo-morphs. But has that been the sum total of our evolutionary history, to be merely little more than overgrown juvenile apes? More recent studies, however, have shown that many of our morphological features are, on the contrary, peramor-phic (see Minugh-Purvis and McNamara2002for a review). The structure at the base of our skull that enables us to walk upright and face forward is nothing at all like any structure in juvenile apes. Our overall large body size, relatively large legs, structure of our pelvis, enlarged crani-um and brain, and even our big feet are peramorphic fea-tures arising from the delay in onset of our maturity (hypermorphosis) compared with ancestral apes. In terms of our extended growth period, we are the late finishers of the ape world. Each part of our development–embryonic, infantile, and juvenile–has been relatively extended, com-pared with our ancestors. Such extension of succeeding growth stages during ontogeny is known as “sequential hypermorphosis” (McNamara 2002) and has been shown to be critical in the evolution of our brain (Rice2002). This prolonged period of pre-adult development has resulted not only in our large body but especially our larger brain, which has allowed a longer period to be spent in the critical phase of learning. We are a classic example of dissociated hetero-chrony, where some peramorphic features are developmen-tal trade-offs for other, paedomorphic, features: some parts of our anatomy are relatively retarded, compared with our ancestors, but others have developed beyond. Arguably, it is these peramorphic features which are the ones that have led to the success of our species on this planet, and all that that entails.
an anonymous referee for their constructive comments on the manuscript.
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